间充质干细胞
SOX2
CD44细胞
川地34
干细胞
脐带
CD90型
男科
干细胞标记物
脐带血
生物
病理
免疫学
医学
胚胎干细胞
细胞生物学
细胞
生物化学
基因
作者
Issam Hussain,Salah A. Magd,Oleg Eremin,Mohamed El‐Sheemy
摘要
Abstract HUCB (human umbilical cord blood) has been frequently used in clinical allogeneic HSC (haemopoietic stem cell) transplant. However, HUCB is poorly recognized as a rich source of MSC (mesenchymal stem cell). The aim of this study has been to establish a new method for isolating large number of MSC from HUCB to recognize it as a good source of MSC. HUCB samples were collected from women following their elective caesarean section. The new method (Clot Spot method) was carried out by explanting HUCB samples in mesencult complete medium and maintained in 37°C, in a 5% CO 2 and air incubator. MSC presence was established by quantitative and qualitative immunophenotyping of cells and using FITC attached to MSC phenotypic markers (CD29, CD73, CD44 and CD105). Haematopoietic antibodies (CD34 and CD45) were used as negative control. MSC differentiation was examined in neurogenic and adipogenic media. Immunocytochemistry was carried out for the embryonic markers: SOX2 (sex determining region Y‐box 2), OLIG‐4 (oligodendrocyte‐4) and FABP‐4 (fatty acid binding protein‐4). The new method was compared with the conventional Rosset Sep method. MSC cultures using the Clot Spot method showed 3‐fold increase in proliferation rate compared with conventional method. Also, the cells showed high expression of MSC markers CD29, CD73, CD44 and CD105, but lacked the expression of specific HSC markers (CD34 and CD45). The isolated MSC showed some differentiation by expressing the neurogenic (SOX2 and Olig4) and adipogenic (FABP‐4) markers respectively. In conclusion, HUCB is a good source of MSC using this new technique.
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